| ID: 127815046 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595901-86596409 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980986..83981494) | | |
| ID: 127815045 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86595393-86595900 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980469..83980985) | | |
| ID: 127815044 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:86577603-86578233 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83962688..83963318) | | |
| ID: 101927575 | uncharacterized LOC101927575 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84063443..84094601) | | |
| ID: 100874474 | high mobility group nucleosomal binding domain 2 pseudogene 33 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (84078517..84079057) | | |
| ID: 407043 | microRNA 7-1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83969748..83969857, complement) | MIRN7-1, hsa-mir-7-1, mir-7-1 | 615239 |
| ID: 84267 | Q-nucleotide N-glycosylase 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83938311..83956986, complement) | C9orf64 | 611342 |
| ID: 80010 | RecQ mediated genome instability 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83980359..84004074) | BLAP75, C9orf76, FAAP75 | 610404 |
| ID: 3190 | heterogeneous nuclear ribonucleoprotein K [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83968083..83980615, complement) | AUKS, CSBP, HNRPK, TUNP | 600712 |